Zimmer Biomet, Inc.: Medical Device Recall in 2018 - (Recall #: Z-0939-2018)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2018.

Data Source: FDA.

Product Description:

Trabecular Metal¿ Primary Hip Prosthesis; Part Numbers: 1. 00-7864-013-00 (UDI: (01) 00889024139251 (17) 250731 (10) 63703649), and 2. 00-7864-013-20 (UDI: (01) 00889024139268 (17) 250731 (10) 63703681)

Product Classification:

Class II

Date Initiated: January 3, 2018

Date Posted: March 21, 2018

Recall Number: Z-0939-2018

Event ID: 79397

Reason for Recall:

Two lots of hip implants are mislabeled.

Status: Terminated

Product Quantity: 24

Code Information:

Part Numbers: 1. 00-7864-013-00, Lot: 63703649; 2. 00-7864-013-20, Lot: 63703681

Distribution Pattern:

Distributed in 2 US states: LA and NY. Distributed in Canada, China, Japan, and Switzerland.

Voluntary or Mandated:

Voluntary: Firm initiated